NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE
K-Number: K911970 · 1992-08-14
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Device Summary
Frequently Asked Questions
What is the NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE?
NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE is a medical device that received FDA 510(k) clearance on 1992-08-14. The listed applicant is Nasorcap Ent., Inc.. The 510(k) number is K911970.
When did NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE receive FDA 510(k) clearance?
NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE received FDA 510(k) clearance on 1992-08-14, under 510(k) number K911970.
Who is the listed applicant for NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE?
The FDA 510(k) record lists Nasorcap Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE?
The FDA product code for NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE is CCK.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CCK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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